Collagenofibrotic glomerulopathy in a kidney transplant recipient: A first report

被引：0

作者：

Jdiaa, Sara S. ^{[1
]}

Moeckel, Gilbert W. ^{[2
]}

Kfoury, Hala M. ^{[3
]}

Medawar, Walid A. ^{[1
]}

Abu-Alfa, Ali K. ^{[1
,4
]}

机构：

[1] Amer Univ Beirut, Fac Med, Dept Internal Med, Div Nephrol & Hypertens, Beirut, Lebanon

[2] Yale Univ, Sch Med, Dept Pathol, Div Renal Pathol & Electron Microscopy, New Haven, CT 06510 USA

[3] Amer Univ Beirut, Fac Med, Dept Pathol & Lab Med, Div Anat Pathol, Beirut, Lebanon

[4] Yale Univ, Sch Med, Dept Internal Med, Sect Nephrol, New Haven, CT USA

来源：

AMERICAN JOURNAL OF TRANSPLANTATION | 2021年 / 21卷 / 05期

关键词：

clinical research; practice; genetics; kidney transplantation; nephrology; recurrent disease; III GLOMERULOPATHY; COLLAGEN; PATELLA;

D O I：

10.1111/ajt.16399

中图分类号：

R61 [外科手术学];

学科分类号：

摘要：

Collagenofibrotic glomerulopathy (CG) is a rare disease characterized by the deposition of collagen type 3 fibrils in the glomeruli. Patients may have proteinuria, hematuria, and/or renal dysfunction. CG is considered a progressive disease with variable rates of progression. The definitive diagnosis is made by electron microscopy with the presence of characteristic subendothelial and mesangial curved, comma-like, banded collagen type 3 fibers of 40-65 nm periodicity. We are reporting the first case of CG in a kidney transplant recipient with kidney disease of unknown cause.

引用

页码：1948 / 1952

页数：5

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